
Clinical Study Coordinator
2 days ago
The Clinical Research Coordinator plays a pivotal role in the planning, implementation, and coordination of clinical research studies. They are responsible for coordinating and managing all aspects of clinical research studies from initiation to closeout.
This involves screening, recruiting, and enrolling eligible participants according to study protocols. The coordinator must obtain informed consent and ensure compliance with regulatory guidelines and institutional policies.
A key aspect of this role is scheduling study visits, performing study assessments, and collecting study data accurately and in a timely manner. Effective communication with study participants, principal investigators, study sponsors, and other study team members is crucial.
- Study Coordination: Coordinate and manage all aspects of clinical research studies from initiation to closeout.
- Participant Recruitment: Screen, recruit, and enroll eligible participants according to study protocols.
- Regulatory Compliance: Obtain informed consent and ensure compliance with regulatory guidelines and institutional policies.
- Data Management: Schedule study visits, perform study assessments, and collect study data accurately and in a timely manner.
This is an exciting opportunity for individuals who are passionate about research and healthcare. If you are detail-oriented, organized, and able to work effectively in a fast-paced environment, we encourage you to apply for this challenging and rewarding role.
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Clinical Research Director
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Chief Clinical Document Developer
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Clinical Quality Assurance Manager
3 days ago
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Lead Clinical Trial Statistician
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Clinical Data Science Manager
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Data Management Specialist
2 days ago
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Clinical and Pharmacovigilance Lead
5 days ago
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Data Scientist
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Senior Clinical Quality Assurance Specialist
10 hours ago
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Clinical Data Integrity Specialist
4 days ago
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